-
1
-
-
0023653232
-
The Drosophila homolog of the mouse mammary oncogene int-1 is identical to the segment polarity gene wingless
-
Rijsewijk F, Schuermann M, Wagenaar E, Parren P, Weigel D, Nusse R. The Drosophila homolog of the mouse mammary oncogene int-1 is identical to the segment polarity gene wingless. Cell 1987;50: 649-57.
-
(1987)
Cell
, vol.50
, pp. 649-657
-
-
Rijsewijk, F.1
Schuermann, M.2
Wagenaar, E.3
Parren, P.4
Weigel, D.5
Nusse, R.6
-
2
-
-
0029772359
-
The mouse Engrailed-1 gene and ventral limb patterning
-
DOI 10.1038/382360a0
-
Loomis CA, Harris E, Michaud J, Wurst W, Hanks M, Joyner AL. The mouse Engrailed-1 gene and ventral limb patterning. Nature 1996;382:360-3. (Pubitemid 26260464)
-
(1996)
Nature
, vol.382
, Issue.6589
, pp. 360-363
-
-
Loomis, C.A.1
Harris, E.2
Michaud, J.3
Wurst, W.4
Hanks, M.5
Joyner, A.L.6
-
3
-
-
0031800728
-
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
-
DOI 10.1038/ng0598-47
-
Dreyer SD, Zhou G, Baldini A, Winterpacht A, Zabel B, Cole W et al. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome. Nat Genet 1998;19:47-50. (Pubitemid 28242021)
-
(1998)
Nature Genetics
, vol.19
, Issue.1
, pp. 47-50
-
-
Dreyer, S.D.1
Zhou, G.2
Baldini, A.3
Winterpacht, A.4
Zabel, B.5
Cole, W.6
Johnson, R.L.7
Lee, B.8
-
4
-
-
0036957091
-
Nail-patella syndrome. Overview on clinical and molecular findings
-
Bongers EM, Gubler MC, Knoers NV. Nail-patella syndrome. Overview on clinical and molecular findings. Pediatr Nephrol 2002;17:703-12.
-
(2002)
Pediatr Nephrol
, vol.17
, pp. 703-712
-
-
Bongers, E.M.1
Gubler, M.C.2
Knoers, N.V.3
-
5
-
-
0036433896
-
Interactions between dorsal-ventral patterning genes lmx1b, engrailed-1 and wnt-7a in the vertebrate limb
-
Chen H, Johnson RL. Interactions between dorsal-ventral patterning genes Imx1b, engrailed-1 and wnt-7a in the vertebrate limb. Int J Dev Biol 2002;46:937-41. (Pubitemid 35364642)
-
(2002)
International Journal of Developmental Biology
, vol.46
, Issue.7
, pp. 937-941
-
-
Chen, H.1
Johnson, R.L.2
-
6
-
-
33845187080
-
Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia
-
DOI 10.1086/509789
-
Bergmann C, Senderek J, Anhuf D, Thiel CT, Ekici AB, PobleteGutierrez P et al. Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSP04) cause autosomal recessive anonychia. Am J Hum Genet 2006;79:1105-9. (Pubitemid 44853482)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.6
, pp. 1105-1109
-
-
Bergmann, C.1
Senderek, J.2
Anhuf, D.3
Thiel, C.T.4
Ekici, A.B.5
Poblete-Gutierrez, P.6
Van, S.M.7
Seelow, D.8
Nurnberg, G.9
Schild, H.H.10
Nurnberg, P.11
Reis, A.12
Frank, J.13
Zerres, K.14
-
7
-
-
33750489078
-
R-spondin1 is essential in sex determination, skin differentiation and malignancy
-
DOI 10.1038/ng1907, PII NG1907
-
Parma P, Radi O, Vidal V, Chaboissier MC, Dellambra E, Valentini S et al. R-spondin 1 is essential in sex determination, skin differentiation and malignancy. Nat Genet 2006;38:1304-9. (Pubitemid 44646293)
-
(2006)
Nature Genetics
, vol.38
, Issue.11
, pp. 1304-1309
-
-
Parma, P.1
Radi, O.2
Vidal, V.3
Chaboissier, M.C.4
Dellambra, E.5
Valentini, S.6
Guerra, L.7
Schedl, A.8
Camerino, G.9
-
8
-
-
35548966679
-
R-Spondin1 regulates Wnt signaling by inhibiting internalization of LRP6
-
DOI 10.1073/pnas.0702305104
-
Binnerts ME, Kim KA, Bright JM, Patel SM, Tran K, Zhou M et al. R-Spondin1 regulates Wnt signaling by inhibiting internalization of LRP6. Proc Natl Acad Sci U S A 2007;104:14700-5. (Pubitemid 350003206)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.37
, pp. 14700-14705
-
-
Binnerts, M.E.1
Kim, K.-A.2
Bright, J.M.3
Patel, S.M.4
Tran, K.5
Zhou, M.6
Leung, J.M.7
Liu, Y.8
Lomas III, W.E.9
Dixon, M.10
Hazell, S.A.11
Wagle, M.12
Nie, W.-S.13
Tomasevic, N.14
Williams, J.15
Zhan, X.16
Levy, M.D.17
Funk, W.D.18
Abo, A.19
-
9
-
-
34447526784
-
R-spondin1 is a high affinity ligand for LRP6 and induces LRP6 phosphorylation and beta-catenin signaling
-
DOI 10.1074/jbc.M701927200
-
Wei Q, Yokota C, Semenov MV, Doble B, Woodgett J, He X. R-spondinl is a high affinity ligand for LRP6 and induces LRP6 phosphorylation and beta-catenin signaling. J Biol Chem 2007;282: 15903-11. (Pubitemid 47093310)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.21
, pp. 15903-15911
-
-
Wei, Q.1
Yokota, C.2
Semenov, M.V.3
Doble, B.4
Woodgett, J.5
He, X.6
-
10
-
-
34247219723
-
The effects of dickkopf 1 on gene expression and wnt signaling by melanocytes: Mechanisms underlying its suppression of melanocyte function and proliferation
-
DOI 10.1038/sj.jid.5700629, PII 5700629
-
Yamaguchi Y, Passeron T, Watabe H, Yasumoto K, Rouzaud F, Hoashi T et al. The effects of Dickkopf 1 on gene expression and WNT signaling by melanocytes: mechanisms underlying its suppression of melanocyte function and proliferation. J Invest Dermatol 2006;127: 1217-25. (Pubitemid 46625128)
-
(2007)
Journal of Investigative Dermatology
, vol.127
, Issue.5
, pp. 1217-1225
-
-
Yamaguchi, Y.1
Passeron, T.2
Watabe, H.3
Yasumoto, K.-I.4
Rouzaud, F.5
Hoashi, T.6
Hearing, V.J.7
-
11
-
-
0033981864
-
An SRY-negative XX male with Huriez syndrome
-
DOI 10.1034/j.1399-0004.2000.570109.x
-
Vernole P, Terrinoni A, Didona B, De Laurenzi V, Rossi P, Melino G et al. An SRY-negative XX male with Huriez syndrome. Clin Genet 2000;57:61-6. (Pubitemid 30105562)
-
(2000)
Clinical Genetics
, vol.57
, Issue.1
, pp. 61-66
-
-
Vernole, P.1
Terrinoni, A.2
Didona, B.3
De, L.V.4
Rossi, P.5
Melino, G.6
Grimaldi, P.7
-
12
-
-
0033925644
-
A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23 [4]
-
DOI 10.1086/302718
-
Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A. A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23. Am J Hum Genet 2000;66:326-30. (Pubitemid 30481494)
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.1
, pp. 326-330
-
-
Lee, Y.-A.1
Stevens, H.P.2
Delaporte, E.3
Wahn, U.4
Reis, A.5
-
13
-
-
67649880580
-
WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
-
Bohring A, Stamm T, Spaich C, Haase C, Spree K, Hehr U et al. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. Am J Hum Genet 2009;85:97-105.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 97-105
-
-
Bohring, A.1
Stamm, T.2
Spaich, C.3
Haase, C.4
Spree, K.5
Hehr, U.6
-
14
-
-
35348987509
-
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia
-
DOI 10.1086/520064
-
Adaimy L, Chouery E, Megarbane H, Mroueh S, Delague V, Nicolas E et al. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Am J Hum Genet 2007;81:821-8. (Pubitemid 47596549)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.4
, pp. 821-828
-
-
Adaimy, L.1
Chouery, E.2
Megarbane, H.3
Mroueh, S.4
Delague, V.5
Nicolas, E.6
Belguith, H.7
De, M.P.8
Megarbane, A.9
-
15
-
-
44149107578
-
New concepts on the histogenesis of eccrine neoplasia from keratin expression in the normal eccrine gland, syringoma and poroma
-
Langbein L, Cribier B, Schirmacher P, Praetzel-Wunder S, Peltre B, Schweizer J. New concepts on the histogenesis of eccrine neoplasia from keratin expression in the normal eccrine gland, syringoma and poroma. Br J Dermatol 2008;159:633-45.
-
(2008)
Br J Dermatol
, vol.159
, pp. 633-645
-
-
Langbein, L.1
Cribier, B.2
Schirmacher, P.3
Praetzel-Wunder, S.4
Peltre, B.5
Schweizer, J.6
-
16
-
-
56749144138
-
Schopf-Schulz-Passarge syndrome: Further delineation of the phenotype and genetic considerations
-
Castori M, Ruggieri S, Giannetti L, Annessi G, Zambruno G. Schopf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations. Acta Derm Venereol 2008;88:607-12.
-
(2008)
Acta Derm Venereol
, vol.88
, pp. 607-612
-
-
Castori, M.1
Ruggieri, S.2
Giannetti, L.3
Annessi, G.4
Zambruno, G.5
-
17
-
-
50449084075
-
Pathological responses to oncogenic Hedgehog signaling in skin are dependent on canonical Wnt/beta3-catenin signaling
-
Yang SH, Andl T, Grachtchouk V, Wang A, Liu J, Syu LJ et al. Pathological responses to oncogenic Hedgehog signaling in skin are dependent on canonical Wnt/beta3-catenin signaling. Nat Genet 2008;40:1130-5.
-
(2008)
Nat Genet
, vol.40
, pp. 1130-1135
-
-
Yang, S.H.1
Andl, T.2
Grachtchouk, V.3
Wang, A.4
Liu, J.5
Syu, L.J.6
-
18
-
-
15844386165
-
Mutations of the human homolog of drosophila patched in the nevoid basal cell carcinoma syndrome
-
DOI 10.1016/S0092-8674(00)81268-4
-
Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A et al. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 1996; 85:841-51. (Pubitemid 26192135)
-
(1996)
Cell
, vol.85
, Issue.6
, pp. 841-851
-
-
Hahn, H.1
Wicking, C.2
Zaphiropoulos, P.G.3
Gailani, M.R.4
Shanley, S.5
Chidambaram, A.6
Vorechovsky, I.7
Holmberg, E.8
Unden, A.B.9
Gillies, S.10
Negus, K.11
Smyth, I.12
Pressman, C.13
Leffell, D.J.14
Gerrard, B.15
Goldstein, A.M.16
Dean, M.17
Toftgard, R.18
Chenevix-Trench, G.19
Wainwright, B.20
Bale, A.E.21
more..
-
19
-
-
0032567078
-
De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin
-
Gat U, DasGupta R, Degenstein L, Fuchs E. De Novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin. Cell 1998;95:605-14. (Pubitemid 28544122)
-
(1998)
Cell
, vol.95
, Issue.5
, pp. 605-614
-
-
Gat, U.1
DasGupta, R.2
Degenstein, L.3
Fuchs, E.4
-
20
-
-
19944433687
-
Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas
-
Reifenberger J, Wolter M, Knobbe CB, Köhler B, Schönicke A, Scharwächter C et al. Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas. Br J Dermatol 2005;152:43-51.
-
(2005)
Br J Dermatol
, vol.152
, pp. 43-51
-
-
Reifenberger, J.1
Wolter, M.2
Knobbe, C.B.3
Köhler, B.4
Schönicke, A.5
Scharwächter, C.6
-
21
-
-
16044363842
-
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
-
DOI 10.1038/ng0996-78
-
Gailani MR, Ståhle-Bäckdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C et al. The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nat Genet 1996;14: 78-81. (Pubitemid 26301550)
-
(1996)
Nature Genetics
, vol.14
, Issue.1
, pp. 78-81
-
-
Gailani, M.R.1
Stahle-Backdahl, M.2
Leffell, D.J.3
Glynn, M.4
Zaphiropoulos, P.G.5
Pressman, C.6
Unden, A.B.7
Dean, M.8
Brash, D.E.9
Bale, A.E.10
Toftgard, R.11
-
22
-
-
0032741860
-
Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
-
Sato N, Leopold PL, Crystal RG. Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog. J Clin Invest 1999;104:855-64. (Pubitemid 29536335)
-
(1999)
Journal of Clinical Investigation
, vol.104
, Issue.7
, pp. 855-864
-
-
Sato, N.1
Leopold, P.L.2
Crystal, R.G.3
-
23
-
-
68249099408
-
Circadian clock genes contribute to the regulation of hair follicle cycling
-
Lin KK, Kumar V, Geyfman M, Chudova D, Ihler AT, Smyth P et al. Circadian clock genes contribute to the regulation of hair follicle cycling. PLoS Genet 2009;5:e1000573.
-
(2009)
PLoS Genet
, vol.5
-
-
Lin, K.K.1
Kumar, V.2
Geyfman, M.3
Chudova, D.4
Ihler, A.T.5
Smyth, P.6
-
24
-
-
0034657419
-
Wnt signaling maintains the hair-inducing activity of the dermal papilla
-
Kishimoto J, Burgeson RE, Morgan BA. Wnt signaling maintains the hair-inducing activity of the dermal papilla. Genes Dev 2000;14:1181-5.
-
(2000)
Genes Dev
, vol.14
, pp. 1181-1185
-
-
Kishimoto, J.1
Burgeson, R.E.2
Morgan, B.A.3
-
25
-
-
0027408032
-
Regulation of wingless transcription in the Drososphila embryo
-
Ingham PW, Hidalgo A. Regulation of wingless transcription in the Drosophila embryo. Development 1993;117:283-91. (Pubitemid 23094175)
-
(1993)
Development
, vol.117
, Issue.1
, pp. 283-291
-
-
Ingham, P.W.1
Hidalgo, A.2
-
26
-
-
0033814577
-
Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling
-
Panteleyev AA, Paus R, Christiano AM. Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling. Am J Pathol 2000;157:1071-9.
-
(2000)
Am J Pathol
, vol.157
, pp. 1071-1079
-
-
Panteleyev, A.A.1
Paus, R.2
Christiano, A.M.3
-
27
-
-
26844523484
-
Hairless triggers reactivation of hair growth by promoting Wnt signaling
-
DOI 10.1073/pnas.0507609102
-
Beaudoin GM 3rd, Sisk JM, Coulombe PA, Thompson CC. Hairless triggers reactivation of hair growth by promoting Wnt signaling. Proc Natl Acad Sci U S A 2005;102:14653-8. (Pubitemid 41457111)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.41
, pp. 14653-14658
-
-
Beaudoin III, G.M.J.1
Sisk, J.M.2
Coulombe, P.A.3
Thompson, C.C.4
-
28
-
-
6844265562
-
Alopecia universalis associated with a mutation in the human hairless gene
-
Ahmad W, Faiyaz ul Haque M, Brancolini V, Tsou HC, ul Haque S, Lam H et al. Alopecia universalis associated with a mutation in the human hairless gene. Science 1998;279:720-4.
-
(1998)
Science
, vol.279
, pp. 720-724
-
-
Ahmad, W.1
Faiyaz Ul Haque, M.2
Brancolini, V.3
Tsou, H.C.4
Ul Haque, S.5
Lam, H.6
-
29
-
-
59149083659
-
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
-
Wen Y, Liu Y, Xu Y, Zhao Y, Hua R, Wang K et al. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. Nat Genet 2009;41:228-33.
-
(2009)
Nat Genet
, vol.41
, pp. 228-233
-
-
Wen, Y.1
Liu, Y.2
Xu, Y.3
Zhao, Y.4
Hua, R.5
Wang, K.6
-
30
-
-
0036113510
-
WNT signals are required for the initiation of hair follicle development
-
DOI 10.1016/S1534-5807(02)00167-3
-
Andl T, Reddy ST, Gaddapara T, Millar SE. WNT signals are required for the initiation of hair follicle development. Dev Cell 2002;2:643-53. (Pubitemid 34538144)
-
(2002)
Developmental Cell
, vol.2
, Issue.5
, pp. 643-653
-
-
Andl, T.1
Reddy, S.T.2
Gaddapara, T.3
Millar, S.E.4
-
31
-
-
0037456847
-
Links between signal transduction, transcription and adhesion in epithelial bud development
-
DOI 10.1038/nature01458
-
Jamora C, DasGupta R, Kocieniewski P, Fuchs E. Links between signal transduction, transcription and adhesion in epithelial bud development. Nature 2003;422:317-22. (Pubitemid 36378359)
-
(2003)
Nature
, vol.422
, Issue.6929
, pp. 317-322
-
-
Jamora, C.1
DasGupta, R.2
Kocieniewski, P.3
Fuchs, E.4
-
32
-
-
0034800098
-
Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene
-
DOI 10.1046/j.0022-202X.2001.01438.x
-
Miller J, Djabali K, Chen T, Liu Y, Ioffreda M, Lyle S et al. Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene. J Invest Dermatol 2001;117:612-7. (Pubitemid 32955588)
-
(2001)
Journal of Investigative Dermatology
, vol.117
, Issue.3
, pp. 612-617
-
-
Miller, J.1
Djabali, K.2
Chen, T.3
Liu, Y.4
Ioffreda, M.5
Lyle, S.6
Christiano, A.M.7
Holick, M.8
Cotsarelis, G.9
-
33
-
-
0035887252
-
The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
-
DOI 10.1101/gad.916701
-
Potter GB, Beaudoin GM 3rd, DeRenzo CL, Zarach JM, Chen SH, Thompson CC et al. The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor. Genes Dev 2001;15:2687-701. (Pubitemid 32988879)
-
(2001)
Genes and Development
, vol.15
, Issue.20
, pp. 2687-2701
-
-
Potter, G.B.1
Beaudoin III, G.M.J.2
DeRenzo, C.L.3
Zarach, J.M.4
Chen, S.H.5
Thompson, C.C.6
-
34
-
-
0141961566
-
Physical and functional interaction between the vitamin D receptor and hairless corepressor, two proteins required for hair cycling
-
Hsieh JC, Sisk JM, Jurutka PW, Haussler CA, Slater SA, Haussler MR et al. Physical and functional interaction between the vitamin D receptor and hairless corepressor, two proteins required for hair cycling. J Biol Chem 2003;278:38665-74.
-
(2003)
J Biol Chem
, vol.278
, pp. 38665-38674
-
-
Hsieh, J.C.1
Sisk, J.M.2
Jurutka, P.W.3
Haussler, C.A.4
Slater, S.A.5
Haussler, M.R.6
-
35
-
-
34548514822
-
Interactions of the vitamin D receptor with the corepressor hairless: Analysis of hairless mutants in atrichia with papular lesions
-
Wang J, Malloy PJ, Feldman D. Interactions of the vitamin D receptor with the corepressor hairless: analysis of hairless mutants in atrichia with papular lesions. J Biol Chem 2007;282:25231-9.
-
(2007)
J Biol Chem
, vol.282
, pp. 25231-25239
-
-
Wang, J.1
Malloy, P.J.2
Feldman, D.3
-
36
-
-
44649160789
-
The vitamin D receptor is a Wnt effector that controls hair follicle differentiation and specifies tumor type in adult epidermis
-
Pálmer HG, Anjos-Afonso F, Carmeliet G, Takeda H, Watt FM. The vitamin D receptor is a Wnt effector that controls hair follicle differentiation and specifies tumor type in adult epidermis. PLoS ONE 2008;3:e1483.
-
(2008)
PLoS ONE
, vol.3
-
-
Pálmer, H.G.1
Anjos-Afonso, F.2
Carmeliet, G.3
Takeda, H.4
Watt, F.M.5
-
37
-
-
55749104413
-
Vitamin D and Wnt/beta-catenin pathway in colon cancer: Role and regulation of DICKKOPF genes
-
Pendás-Franco N, Aguilera O, Pereira F, González-Sancho JM, Muñoz A. Vitamin D and Wnt/beta-catenin pathway in colon cancer: role and regulation of DICKKOPF genes. Anticancer Res 2008;28: 2613-23.
-
(2008)
Anticancer Res
, vol.28
, pp. 2613-2623
-
-
Pendás-Franco, N.1
Aguilera, O.2
Pereira, F.3
González-Sancho, J.M.4
Muñoz, A.5
-
38
-
-
34848858270
-
3 associated to the differentiation of human colon cancer cells
-
DOI 10.1093/carcin/bgm094
-
Aguilera O, Peña C, García JM, Larriba MJ, Ordóñez-Morán P, Navarro D et al. The Wnt antagonist DICKKOPF-1 gene is induced by 1 alpha,25-dihydroxyvitamin D3 associated to the differentiation of human colon cancer cells. Carcinogenesis 2007;28:1877-84. (Pubitemid 47500598)
-
(2007)
Carcinogenesis
, vol.28
, Issue.9
, pp. 1877-1884
-
-
Aguilera, O.1
Pena, C.2
Garcia, J.M.3
Larriba, M.J.4
Ordonez-moran, P.5
Navarro, D.6
Barbachano, A.7
De, S.I.L.8
Ballestar, E.9
Fraga, M.F.10
Esteller, M.11
Gamallo, C.12
Bonilla, F.13
Gonzalez-Sancho, J.M.14
Munoz, A.15
-
39
-
-
33947103125
-
3 induces expression of the Wnt signaling co-regulator LRP5 via regulatory elements located significantly downstream of the gene's transcriptional start site
-
DOI 10.1016/j.jsbmb.2006.11.018, PII S0960076006003669
-
Fretz JA, Zella LA, Kim S, Shevde NK, Pike JW. 1,25-Dihydroxyvitamin D3 induces expression of the Wnt signaling co-regulator LRP5 via regulatory elements located significantly downstream of the gene's transcriptional start site. J Steroid Biochem Mol Biol 2007;103:440-5. (Pubitemid 46401288)
-
(2007)
Journal of Steroid Biochemistry and Molecular Biology
, vol.103
, Issue.3-5
, pp. 440-445
-
-
Fretz, J.A.1
Zella, L.A.2
Kim, S.3
Shevde, N.K.4
Pike, J.W.5
-
40
-
-
33747332214
-
Repression of smoothened by patched-dependent (pro-)vitamin D3 secretion
-
Bijlsma MF, Spek CA, Zivkovic D, van de Water S, Rezaee F, Peppelenbosch MP. Repression of smoothened by patched-dependent (pro-)vitamin D3 secretion. PLoS Biol 2006;4:e232.
-
(2006)
PLoS Biol
, vol.4
-
-
Bijlsma, M.F.1
Spek, C.A.2
Zivkovic, D.3
Van De Water, S.4
Rezaee, F.5
Peppelenbosch, M.P.6
-
41
-
-
46149115894
-
Incorporation of histone deacetylase inhibition into the structure of a nuclear receptor agonist
-
DOI 10.1073/pnas.0709279105
-
Tavera-Mendoza LE, Quach TD, Dabbas B, Hudon J, Liao X, Palijan A et al. Incorporation of histone deacetylase inhibition into the structure of a nuclear receptor agonist. Proc Natl Acad Sci U S A 2008;105:8250-5. (Pubitemid 351904740)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.24
, pp. 8250-8255
-
-
Tavera-Mendoza, L.E.1
Quach, T.D.2
Dabbas, B.3
Hudon, J.4
Liao, X.5
Palijan, A.6
Gleason, J.L.7
White, J.H.8
|